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磁共振引导高强度聚焦超声(MRgHIFU)介导的盆腔靶区温和热疗的可行性和安全性评估:使用猪模型进行评估。

Feasibility and safety assessment of magnetic resonance-guided high-intensity focused ultrasound (MRgHIFU)-mediated mild hyperthermia in pelvic targets evaluated using an porcine model.

机构信息

Department of Biomedical Engineering, Washington University in St. Louis, St. Louis, MO, USA.

Clinical Science, Profound Medical Inc., Mississauga, ON, Canada.

出版信息

Int J Hyperthermia. 2019;36(1):1147-1159. doi: 10.1080/02656736.2019.1685684.

Abstract

To evaluate the feasibility and assess safety parameters of magnetic resonance-guided high-intensity focused ultrasound (MRgHIFU)-mediated hyperthermia (HT; heating to 40-45 °C) in various pelvic targets in a porcine model . Thirteen HT treatments were performed in six pigs with a commercial MRgHIFU system (Sonalleve V2, Profound Medical Inc., Mississauga, Canada) to muscle adjacent to the ventral/dorsal bladder wall and uterus to administer 42 °C (±1°) for 30 min (±5%) using an 18-mm target diameter and 100 W power. Feasibility was assessed using accuracy, uniformity, and MR-thermometry performance-based metrics. Safety parameters were assessed for tissues in the targets and beam-path by contrast-enhanced MRI, gross-pathology and histopathology. Across all HT sessions, the mean difference between average temperature (T) and the target temperature within the target region-of-interest (tROI, the cross-section of the heated volume at focal depth) was 0.51 ± 0.33 °C. Within the tROI, the temperature standard deviation averaged 1.55 ± 0.31 °C, the average 30-min T variation was 0.80 ± 0.17 °C, and the maximum difference between T and the 10th- or 90th-percentile temperature averaged 2.01 ± 0.44 °C. The average time to reach ≥41 °C and cool to ≤40 °C within the tROI at the beginning and end of treatment was 47.25 ± 27.47 s and 66.37 ± 62.68 s, respectively. Compared to unheated controls, no abnormally-perfused tissue or permanent damage was evident in the MR images, gross pathology or histological analysis. MRgHIFU-mediated HT is feasible and safety assessment is satisfactory for treating an array of clinically-mimicking pelvic geometries in a porcine model , implying the technique may have utility in treating pelvic targets in human patients.

摘要

评估磁共振引导高强度聚焦超声(MRgHIFU)介导的热疗(HT;加热至 40-45°C)在猪模型中各种盆腔靶标中的可行性,并评估安全性参数。使用商业 MRgHIFU 系统(加拿大密西沙加市 Profound Medical Inc. 的 Sonalleve V2)在 6 头猪中进行了 13 次 HT 治疗,将肌肉与腹/背侧膀胱壁和子宫相邻,将 42°C(±1°C)施加 30 分钟(±5%),使用 18-mm 靶直径和 100 W 功率。使用基于准确性、均匀性和磁共振测温性能的指标来评估可行性。通过对比增强 MRI、大体病理学和组织病理学评估靶标和射束路径中的组织安全性参数。在所有 HT 治疗中,目标区域内平均温度(T)与目标温度之间的平均差异为 0.51±0.33°C。在 tROI 内,温度标准差平均为 1.55±0.31°C,平均 30 分钟 T 变化为 0.80±0.17°C,T 与第 10 或 90 百分位数温度之间的最大差异平均为 2.01±0.44°C。在治疗开始和结束时,tROI 内达到≥41°C 并冷却至≤40°C 的平均时间分别为 47.25±27.47s 和 66.37±62.68s。与未加热的对照组相比,MR 图像、大体病理学或组织学分析均未显示异常灌注组织或永久性损伤。MRgHIFU 介导的 HT 是可行的,安全性评估令人满意,可用于治疗猪模型中一系列临床模拟的盆腔几何形状,这意味着该技术可能在治疗人类患者的盆腔靶标方面具有应用价值。

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